Canonical Allele Identifier: CA399313582

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884089T>G (hg19) ; chr17:g.39727836T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727836T>G , CM000679.2:g.39727836T>G	GRCh38
NC_000017.10:g.37884089T>G , CM000679.1:g.37884089T>G	GRCh37
NC_000017.9:g.35137615T>G	NCBI36
NG_007503.1:g.44697T>G , LRG_724:g.44697T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3560T>G MANE Select	ENSP00000269571.4:p.Phe1187Cys
ENST00000269571.9:c.3560T>G	ENSP00000269571.4:p.Phe1187Cys
ENST00000406381.6:c.3470T>G	ENSP00000385185.2:p.Phe1157Cys
ENST00000445658.6:c.2732T>G	ENSP00000404047.2:p.Phe911Cys
ENST00000541774.5:c.3515T>G	ENSP00000446466.1:p.Phe1172Cys
ENST00000578373.5:c.*3350T>G	ENSP00000463427.1:n.*3350T>G
ENST00000584450.5:c.*139T>G	ENSP00000463714.1:n.*139T>G
ENST00000584601.5:c.3470T>G	ENSP00000462438.1:p.Phe1157Cys
NM_001005862.2:c.3470T>G , LRG_724t1:c.3470T>G	NP_001005862.1:p.Phe1157Cys
NM_001289936.1:c.3515T>G , LRG_724t4:c.3515T>G	NP_001276865.1:p.Phe1172Cys
NM_001289937.1:c.*139T>G	NP_001276866.1:n.*139T>G
NM_004448.3:c.3560T>G , LRG_724t2:c.3560T>G	NP_004439.2:p.Phe1187Cys
NR_110535.1:n.3884T>G
XM_024450641.1:c.3698T>G	XP_024306409.1:p.Phe1233Cys
XM_024450642.1:c.3653T>G	XP_024306410.1:p.Phe1218Cys
XM_024450643.1:c.3608T>G	XP_024306411.1:p.Phe1203Cys
NM_001005862.3:c.3470T>G	NP_001005862.1:p.Phe1157Cys
NM_001289936.2:c.3515T>G	NP_001276865.1:p.Phe1172Cys
NM_001289937.2:c.*139T>G	NP_001276866.1:n.*139T>G
NM_001382782.1:c.3470T>G	NP_001369711.1:p.Phe1157Cys
NM_001382783.1:c.3470T>G	NP_001369712.1:p.Phe1157Cys
NM_001382784.1:c.3677T>G	NP_001369713.1:p.Phe1226Cys
NM_001382785.1:c.3662T>G	NP_001369714.1:p.Phe1221Cys
NM_001382786.1:c.3641T>G	NP_001369715.1:p.Phe1214Cys
NM_001382787.1:c.3635T>G	NP_001369716.1:p.Phe1212Cys
NM_001382788.1:c.3590T>G	NP_001369717.1:p.Phe1197Cys
NM_001382789.1:c.3581T>G	NP_001369718.1:p.Phe1194Cys
NM_001382790.1:c.3557T>G	NP_001369719.1:p.Phe1186Cys
NM_001382791.1:c.3551T>G	NP_001369720.1:p.Phe1184Cys
NM_001382792.1:c.3524T>G	NP_001369721.1:p.Phe1175Cys
NM_001382793.1:c.3518T>G	NP_001369722.1:p.Phe1173Cys
NM_001382794.1:c.3518T>G	NP_001369723.1:p.Phe1173Cys
NM_001382795.1:c.3512T>G	NP_001369724.1:p.Phe1171Cys
NM_001382796.1:c.3473T>G	NP_001369725.1:p.Phe1158Cys
NM_001382797.1:c.3461T>G	NP_001369726.1:p.Phe1154Cys
NM_001382798.1:c.3404T>G	NP_001369727.1:p.Phe1135Cys
NM_001382799.1:c.3380T>G	NP_001369728.1:p.Phe1127Cys
NM_001382800.1:c.3374T>G	NP_001369729.1:p.Phe1125Cys
NM_001382801.1:c.3356T>G	NP_001369730.1:p.Phe1119Cys
NM_001382802.1:c.3302T>G	NP_001369731.1:p.Phe1101Cys
NM_001382803.1:c.*139T>G	NP_001369732.1:n.*139T>G
NM_001382804.1:c.2732T>G	NP_001369733.1:p.Phe911Cys
NM_001382805.1:c.2609T>G	NP_001369734.1:p.Phe870Cys
NM_001382806.1:c.2522T>G	NP_001369735.1:p.Phe841Cys
NM_004448.4:c.3560T>G MANE Select	NP_004439.2:p.Phe1187Cys
NR_110535.2:n.3798T>G